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"6,7,14,15,22,23-hexaoxatrispiro[4.2.5~8~.2.5~16~.2~5~]tricosane" is a complex organic compound characterized by its unique molecular structure. It consists of a tricosane backbone, which is a 23-carbon alkane chain, with six oxygen atoms incorporated into the molecule, creating six oxirane (epoxy) rings. These rings are arranged in a spiro configuration, meaning they are interconnected in a cyclic manner, with the carbon atoms at positions 6, 7, 14, 15, 22, and 23 being part of the spiro linkages. The compound's name reflects its molecular formula and structure, indicating the specific arrangement of the carbon and oxygen atoms. This type of compound is typically synthesized in the laboratory and may have applications in various fields, such as pharmaceuticals or materials science, due to its specific chemical properties and potential reactivity.

6789-46-4

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6789-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6789-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6789-46:
(6*6)+(5*7)+(4*8)+(3*9)+(2*4)+(1*6)=144
144 % 10 = 4
So 6789-46-4 is a valid CAS Registry Number.

6789-46-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7,14,15,22,23-hexaoxatrispiro[4.2.5<sup>8</sup>.2.5<sup>16</sup>.2<sup>5</sup>]tricosane

1.2 Other means of identification

Product number -
Other names Dicyclohexyliden-cyclopentyliden-triperoxid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6789-46-4 SDS

6789-46-4Relevant academic research and scientific papers

Flow Chemistry under Extreme Conditions: Synthesis of Macrocycles with Musklike Olfactoric Properties

Seemann, Alexandra,Panten, Johannes,Kirschning, Andreas

, p. 13924 - 13933 (2021/05/29)

Starting from small cyclic ketones, continuous flow synthesis is used to produce medium-sized rings and macrocycles that are relevant for the fragrance industry. Triperoxides are important intermediates in this process and are pyrolyzed at temperatures above 250 °C. The synthesis is carried out in two continuously operated flow reactors connected by a membrane-operated separator. The practicality of flow chemistry is impressively demonstrated in this work by the use of hazardous reagent mixtures (30% H2O2, 65% HNO3) and the pyrolysis of no less problematic peroxides. All new macrocycles were tested for their olfactory properties in relation to musk.

New preparation of 1,2,4,5,7,8-hexaoxonanes

Terent'ev, Alexander O.,Platonov, Maxim M.,Sonneveld, Eduard J.,Peschar, Rene,Chernyshev, Vladimir V.,Starikova, Zoya A.,Nikishin, Gennady I.

, p. 7237 - 7243 (2008/02/12)

(Chemical Equation Presented) A new versatile procedure was developed for the synthesis of 1,2,4,5,7,8-hexaoxonanes based on the Lewis acid catalyzed reaction of acetals with 1,1′-dihydroperoxydicycloalkyl peroxides. The procedure substantially extends the structural diversity of these compounds and, in most cases, allows the synthesis of these compounds in higher yields (to 96%) and with higher selectivity. Complexation of hexaoxonane with chloroform was documented for the first time. The structures of several triperoxides were established by X-ray diffraction.

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